[0001] This invention relates generally to improvements relating to hygiene and medical
products. The invention is particularly suitable for personal hygiene projects such
as ostomy bags, but the invention is not limited exclusively to such use.
[0002] The conventional approach to the manufacture of ostomy bags has been to use a material
which is impermeable to gas, in order to prevent unpleasant odours from leaking by
seepage of gas through the bag wall. Such odours are present in flatus, and are also
produced by bacterial action in decomposing faecal matter. The human nose is extremely
sensitive to such odours (usually caused by hydrogen sulphide gas), and it is critical
for customer acceptance that no unpleasant odours be allowed to escape while the bag
is worn. Typically, a vent with a filter is provided through which filtered gas can
escape to avoid the build up of gas within the bag. However, the effect of the filter
will be wasted if even small amounts of odour-carrying gas are permitted to seep through
the bag walls.
[0003] In order to achieve the necessary gas-impermeability, a gas-impermeable barrier layer
is usually included in the plastics laminate constituting the bag wall material. The
most common, and effective, barrier material is polyvinylidene chloride (PVDC). However,
PVDC is expensive, and is a difficult material to handle. There are growing safety
and environmental concerns regarding the safe disposal of PVDC, particularly by incineration.
Moreover, PVDC has a highly crystalline structure, which makes the laminate "noisy"
in the sense that the material will crackle or rustle when it moves, or is bent, or
slides under a person's clothing. Such noises can be embarrassing for the wearer of
the bag.
[0004] The present invention has been devised bearing such problems in mind.
[0005] In a first aspect, the invention provides a container for carrying or collecting
odorous material, wherein the container carries or contains microencapsulated malodour
counteractant material.
[0006] In a closely-related second aspect, the invention provides an ostomy bag carrying
or containing microencapsulated malodour counteractant material.
[0007] The invention can alleviate the need to provide a gas-impermeable barrier layer (e.g.
of PVDC) in the wall material of the container. Instead, wall material can be used
which does allow permeation of gas through the wall. The malodour counteractant is
released and is able to counter the unpleasant odour within the bag. Therefore, any
gas which does permeate through the container wall will not have an unpleasant odour.
[0008] Microencapsulation is a known technique in which a very small quantity of a material
is encapsulated within a layer, or skin of encapsulant material. In the present case
encapsulation traps the malodour counteractant material, thereby preserving its state
and preventing dispersal or substantial decay of its malodour counteractant properties.
The encapsulant is such that it is able to release the encapsulated material, for
example, by mechanical rupture, temperature dependent release, or moisture-activated
release. This can provide controlled, progressive release of the malodour counteractant
to provide continued odour suppression.
[0009] Microencapsulation has been used in the past to provide so-called "scratch and sniff"
smells. Small quantities of a fragrance are encapsulated within an encapsulant material,
usually gelatin based, which is then applied to card or paper. When the microencapsulated
material is scratched or rubbed, the gelatin skin ruptures, releasing the fragrance.
[0010] The microencapsulated malodour counteractant may, for example, be carried on an interior
face of a wall of the bag or container. Preferably, the microencapsulated material
is carried on the faces of a plurality of walls, more preferably on the interior faces
of all of the bag walls.
[0011] In the case of a container or bag which has walls welded together along one or more
seams, the microencapsulated material may be carried over most of the interior face
of the bag wall except the region of the weld. The microencapsulated material might
otherwise interfere with the weld around the periphery.
[0012] In addition to, or as an alternative to, the microencapsulated material being carried
on the wall of the bag or container, the microencapsulated material may be carried
on an article placed within the bag or container. For example, the microencapsulated
material may be carried on an absorbent or a superabsorbent article, such as that
described in GB-A-2,301,350.
[0013] In a closely-related aspect, the invention provides a product for insertion in an
ostomy bag, the product carrying microencapsulated malodour counteractant material.
[0014] In a further closely-related aspect, the invention provides a product comprising
super-absorbent material and microencapsulated malodour counteractant material.
[0015] In a further closely-related aspect, the invention provides a medical or hygiene
product carrying or containing a microencapsulated active material such that, in use,
the active material is releasable from the microencapsulated state.
[0016] The term "active material" is intended to cover any material providing a medical
or hygiene function, in use. For example, such materials include malodour counteractants,
medicaments, and disinfectants.
[0017] In a closely related aspect, the invention provides a container for containing or
collecting unpleasantly odorous material, the container having at least one wall made
of material which is at least partly permeable to gas, the container carrying or containing
a malodour counteractant material to counter the unpleasant odour of gas leaking through
the container wall.
[0018] Preferably, the container further comprises a vent providing a main gas escape path
for gas.
[0019] The term "at least partly permeable" is intended to refer to the material being such
that at least some gas can leak through the wall in sufficient quantity to produce
a detectable unpleasant odour outside the container, were it not for the presence
of the malodour counteractant.
[0020] Preferably, the container is an ostomy bag.
[0021] In a closely-related further aspect, the invention provides a method of applying
a malodour counteractant to a product for ostomy use, the method comprising applying
the malodour counteractant in a microencapsulated state.
[0022] In a yet further closely related aspect, the invention provides a method of applying
an active material to a medical or hygiene product, the method comprising applying
the active material in a microencapsulated state.
[0023] In the above methods, the microencapsulated material may be solution coated onto
the product, or it may be "printed" by any suitable printing technique, such as silk
screen printing, tampo-offset printing, or ink-jet printing.
[0024] Embodiments of the invention are now described by way of example only, with reference
to the accompanying drawings, in which:-
Figure 1 is a schematic section through an ostomy bag embodying the invention;
Figure 2 is a schematic view showing activation of the counteractant material used
in Figure 1;
Figures 3 and 4 are views showing the areas of application of the malodour counteractant
during production of the ostomy bag;
Figure 5 is an enlarged view showing a detail of Figure 1; and
Figure 6 is a schematic view of an absorbent product carrying microencapsulated malodour
counteractant, for insertion in an ostomy bag.
[0025] Referring to Figures 1 and 2, an ostomy bag consists of a front wall 10 and a rear
wall 12 welded together around their periphery to form a welded seam 14. In this embodiment,
the front and rear walls are made of the same plastics material. In contrast to the
prior art, in this embodiment the wall material does not need to be impermeable to
gas, and it does not require the presence of a gas-impenetrable barrier layer. The
wall may be of any suitable of mono-layer or laminate, plastics film material, such
as thermoplastic elastomers, polyetherurythanes and polyolefins.
[0026] In an upper region, the rear wall 12 has a stomal orifice 16 which is surrounded
by a coupling member 18 on the exterior of the bag. In use, the coupling member 18
enables the bag to be coupled to a body-side coupling member 20 (Fig. 2) worn on the
ostomate's peristomal area. Typically, the coupling parts are held together by adhesive
or by a mechanical locking arrangement.
[0027] In an upper region, the front wall 10 has a vent aperture 22 over which a filter
element 24 (for example of activated charcoal) and a perforated cover 26 are sealed.
The vent enables excess gas in the bag to escape, to prevent a build up of gas and
thereby pressure inside the ostomy bag. Although the bag wall is of a material which
is at least partly permeable to gas, the rate of gas transpiration through the wall
material will generally not be sufficient to allow all of the gas to escape. Typically,
the amount of gas entering the bag through the stomal orifice can be as much as 100
millilitres per minute, on an intermittent basis.
[0028] In accordance with the principles of one aspect of the invention, the ostomy bag
carries or contains a malodour counteractant. The purpose of the malodour counteractant
is to absorb the unpleasant odour in the bag, or to modify or mask the odour with
a counter-fragrance. Thus, the unpleasantness of the odour in the bag can be reduced,
such that any gas leaking through the material of the walls 10 and 12 will not cause
unpleasant smells.
[0029] In the present embodiment, the malodour counteractant is provided in a microencapsulated
form (depicted by numeral 28) and is carried on the interior faces of the front and
rear walls 10 and 12. Referring to Figure 5, the counteractant material is encapsulated
as micro-spheres or beads 30 which are surrounded by a skin or layer 32 of encapsulant
material.
[0030] Microencapsulation is a known technique in which very small globules or beads of
material, usually of the order of a few microns in size, are surrounded by a coating
or skin of encapsulant. The encapsulant traps the material preserving its state and
preventing the material from dispersing. The material can be released from the encapsulant
at an appropriate time by any suitable method depending on the encapsulant material.
For example, release may occur in response to mechanical disturbance or rupture of
the encapsulant, or to chemical breakdown, or to contact with moisture (e.g. by dissolving
the encapsulant) or to temperature (e.g. by melting of the encapsulant).
[0031] The encapsulant may be solid. Alternatively, the encapsulant may be of an interphase
material, such as gelatine based material, or gum composites, or a combination tailored
to suit the material being encapsulated. The encapsulant may also be tailored to suit
the material on which the microencapsulated beads are carried, to adhere to the surface
of the carrier material. Referring to Figure 5, the bag wall material may, if desired,
be a monolayer (as shown), or it may be a laminate having a surface layer (shown schematically
by broken line 38) to which the encapsulant material will adhere.
[0032] The material within the beads may be solid, or it may be fluid, for example, an oil
based or water based liquid, or a gas.
[0033] One technique for preparing microencapsulated material is to emulsify a fluid material
to be encapsulated (e.g. an oil based material) with encapsulant fluid, to produce
the microspheres or beads at the liquid phase interface. The suspended microencapsulated
material can then be applied to a surface on which it is to be carried, by any suitable
application technique. For example, the microencapsulated material may be solution
coated directly onto the plastics film, using a suitable solvent (for example, water).
After drying, this would leave a thin uniform dispersion of microspheres on the plastics
film surface.
[0034] Alternatively, the microspheres may be applied to the surface in a uniform or random
matrix or array using printing techniques, such as screen printing, tampo-offset printing,
or ink-jet printing.
[0035] An example of an oil-based malodour counteractant is the product "Linador" (trade
name) produced by Haarmann & Reimer of Holzminden, Germany.
[0036] Many techniques are known for creating and applying microencapsulated material. For
example, the reader is referred to US-A-4,303,432 and WO-A80/00439 (Microcel Technology,
Inc.).
[0037] In the present embodiment, the microencapsulated malodour counteractant material
is applied over substantially the entire area of the walls 10 and 12, except in predetermined
areas required for welding to form the finished ostomy bag. The microencapsulated
material is omitted from these areas as it might interfere with the integrity or strength
of the welds, and might also cause unwanted release of malodour counteractant during
the welding process. In Figures 3 and 4, the cross-matched areas 40 represent the
area over which the microencapsulant material is applied. In particular, a peripheral
region 42 of both the front wall 10 and the rear wall 12 is left clear for welding
the seam 14, as are an annular region 44 surrounding the vent aperture 22 to which
the cover 26 is welded, and an annular region 46 surrounding the stoma aperture 16
to which the coupling member 18 is welded.
[0038] In use, the microencapsulation of the malodour counteractant prevents the counteractant
material from dispersing and wasting away prior to use of the ostomy bag. When the
bag is worn by an ostomate, and faecal matter (illustrated by numeral 50 in Fig. 2)
enters the bag and contacts the bag wall, the microencapsulant can be activated by
any suitable release mechanism depending on the material of the microencapsulant (e.g.
by temperature, moisture, mechanical rupture) to release the malodour counteractant,
as illustrated schematically at 52. The microencapsulation enables the release of
malodour counteractant to be controlled in relation to the contact area between the
faecal matter and the bag wall. Thus, release of the malodour counteractant can be
controlled to some extent by the amount of faecal matter in the bag, and the rate
of arrival of faecal matter. In particular, the counteractant material can be released
progressively as more faecal matter is collected and contacts more area of the bag
wall.
[0039] If desired an absorbent article 54 (Fig. 1) may be placed inside the ostomy bag to
absorb liquid. For example, the article 54 may include superabsorbent material, such
as that described in our UK Patent Application GB-A-2,301,350. Referring to Figure
6, the article 54 may also carry malodour counteractant, for example, in microencapsulated
form, as depicted by spheres 56. In the Figure 6 embodiment, the absorbent article
54 consists of consolidated superabsorbent powder 58 carried between upper and lower
tissues 60 and 62 respectively. The microencapsulated superabsorbent is applied to
the upper tissue 60, but it could be applied to either or both tissues as required.
[0040] In very general terms, the malodour counteractant may be provided in a non-microencapsulated
form, and have the same function of absorbing or masking unpleasant odours which may
leak through the wall material of the bag. The malodour counteractant could, for example,
be provided in the form of a strip, or tablet, or other article placed inside the
bag. However, microencapsulation enables the counteractant material to be provided
in a form having a large surface area, and which can achieve controlled release of
the malodour counteractant.
[0041] Although the above embodiments illustrate the invention in the field of ostomy, it
will be appreciated that the invention has broader applications. For example, the
invention may be used in any hygiene or medical product in which the controlled release
of an active material, such as a malodour counteractant, medicament, or disinfectant,
is required.
[0042] Although features believed to be of particular importance have been identified in
the foregoing description and in the appended claims, the Applicant claims protection
for any novel feature or combination of features described herein and/or illustrated
in the accompanying drawings.
1. An ostomy bag carrying or containing microencapsulated malodour counteractant material.
2. A container for carrying or collecting odorous material, wherein the container carries
or contains microencapsulated malodour counteractant material.
3. A container or bag according to claim 1 or 2, wherein the container or bag has a wall
or walls through which odorous gas may transpire.
4. A container or bag according to claim 1, 2 or 3, further comprising a vent for allowing
gas to escape, and a filter for filtering odours from gas passing through the vent.
5. A container or bag according to claim 1, 2, 3, or 4, wherein the microencapsulated
malodour counteractant material is carried on an interior face of a wall of the bag
or container.
6. A container or bag according to claim 5, wherein the microencapsulated malodour counteractant
material is carried on the majority of the surface area of the interior face or faces
of the confining walls.
7. A container or bag according to claim 5 or 6, comprising a welded region and wherein
the microencapsulated malodour counteractant material is clear of the welded region.
8. A container or bag according to any preceding claim, wherein the microencapsulated
malodour counteractant material is carried on an article placed within the bag or
container.
9. A product for insertion in an ostomy bag, the product carrying microencapsulated malodour
counteractant material.
10. A product comprising a superabsorbent material and microencapsulated malodour counteractant
material.
11. A medical or hygiene product carrying or containing a microencapsulated active material
such that, in use, the active material is releasable from the microencapsulated state.
12. A container for containing or collecting unpleasantly odorous material, the container
having at least one wall of a material which is at least partly permeable to gas,
the container carrying or containing a malodour counteractant material to counter
the unpleasant odour of gas leaking through the container wall.
13. A container according to claim 12, further comprising a gas vent for providing a main
gas escape path for gas, and a filter for filtering gas flowing through the vent.
14. A method of applying a malodour counteractant to a product for ostomy use, the method
comprising applying the malodour counteractant in microencapsulated form.
15. A method according to claim 14, wherein the microencapsulated malodour counteractant
is applied to a surface of a material which, in use, forms an interior face of a wall
of an ostomy bag.
16. A method of applying an active material to a medical or hygiene product, the method
comprising supplying the active material in a microencapsulated state.